Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,489 recalls have been distributed to Mississippi in the last 12 months.
Showing 21921–21940 of 49,744 recalls
Recalled Item: Centricity PACS Foundation Centricity PACS software product is intended for...
The Issue: There is the possibility of viewing studies directly from the Enterprise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immulox Recalled by APS BioGroup, Inc Due to The recall is being conducted...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DPS Throat Spray Recalled by APS BioGroup, Inc Due to The recall is being...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Viralox Recalled by APS BioGroup, Inc Due to The recall is being conducted...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Immuno PRP Spray Recalled by APS BioGroup, Inc Due to The recall is being...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 45cm Shaft PRODUCT CODE: NSLX145C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 37cm Shaft PRODUCT CODE: NSLX137C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InterStim(TM) System Recalled by Medtronic Neuromodulation Due to There is a...
The Issue: There is a potential for an unexpected increase in stimulation during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntraClude Intra-Aortic Occlusion Device Recalled by Edwards Lifesciences,...
The Issue: Possibility of balloon rupture in intra-aortic occlusion devices. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...
The Issue: GMP Deviations; possible cross contamination of product due to cleaning...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...
The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...
The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Microtainer PSTTubes with LH (Lithium Heparin) Part/Catalog Number:365985...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer SST- Amber Part/Catalog Number: 365978 Recalled by Becton...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer SST Part/Catalog No.365967 Recalled by Becton Dickinson &...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer PST Tubewith LH (Lithium Heparin) - Amber Part/Catalog...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.